Abstract:Combinatorial laser molecular-beam epitaxy method was employed to fabricate epitaxial Zn1−xMnxO thin films in a high throughput fashion. Local structures around Mn were investigated for these c-axis-oriented epitaxial films by fluorescence x-ray absorption fine structure measurements. It was shown that Mn substitutionally replaces Zn in Zn1−xMnxO (x<0.22) films. Well-structured blue and ultraviolet cathodoluminescence peaks corresponding to the intra-d-shell transitions of Mn2+ were observed, especially… Show more
“…All data were corrected for the diamagnetism of the substrate and sample holder. Figure 1a shows electronic absorption spectra of a 0.10 M DMSO solution of 2% 17,22,37,38 The solid line in Figure 1a shows the spectrum collected after 1.65 equiv of base were added. Base addition beyond ca.…”
Abstract:We report the synthesis of colloidal Mn 2+ -doped ZnO (Mn 2+ :ZnO) quantum dots and the preparation of room-temperature ferromagnetic nanocrystalline thin films. Mn 2+ :ZnO nanocrystals were prepared by a hydrolysis and condensation reaction in DMSO under atmospheric conditions. Synthesis was monitored by electronic absorption and electron paramagnetic resonance (EPR) spectroscopies.Zn(OAc) 2 was found to strongly inhibit oxidation of Mn 2+ by O 2 , allowing the synthesis of Mn 2+ :ZnO to be performed aerobically. Mn 2+ ions were removed from the surfaces of as-prepared nanocrystals using dodecylamine to yield high-quality internally doped Mn 2+ :ZnO colloids of nearly spherical shape and uniform diameter (6.1 ± 0.7 nm). Simulations of the highly resolved X-and Q-band nanocrystal EPR spectra, combined with quantitative analysis of magnetic susceptibilities, confirmed that the manganese is substitutionally incorporated into the ZnO nanocrystals as Mn 2+ with very homogeneous speciation, differing from bulk Mn 2+ :ZnO only in the magnitude of D-strain. Robust ferromagnetism was observed in spin-coated thin films of the nanocrystals, with 300 K saturation moments as large as 1.35 µ B /Mn 2+ and T C > 350 K. A distinct ferromagnetic resonance signal was observed in the EPR spectra of the ferromagnetic films. The occurrence of ferromagnetism in Mn 2+ :ZnO and its dependence on synthetic variables are discussed in the context of these and previous theoretical and experimental results.
“…All data were corrected for the diamagnetism of the substrate and sample holder. Figure 1a shows electronic absorption spectra of a 0.10 M DMSO solution of 2% 17,22,37,38 The solid line in Figure 1a shows the spectrum collected after 1.65 equiv of base were added. Base addition beyond ca.…”
Abstract:We report the synthesis of colloidal Mn 2+ -doped ZnO (Mn 2+ :ZnO) quantum dots and the preparation of room-temperature ferromagnetic nanocrystalline thin films. Mn 2+ :ZnO nanocrystals were prepared by a hydrolysis and condensation reaction in DMSO under atmospheric conditions. Synthesis was monitored by electronic absorption and electron paramagnetic resonance (EPR) spectroscopies.Zn(OAc) 2 was found to strongly inhibit oxidation of Mn 2+ by O 2 , allowing the synthesis of Mn 2+ :ZnO to be performed aerobically. Mn 2+ ions were removed from the surfaces of as-prepared nanocrystals using dodecylamine to yield high-quality internally doped Mn 2+ :ZnO colloids of nearly spherical shape and uniform diameter (6.1 ± 0.7 nm). Simulations of the highly resolved X-and Q-band nanocrystal EPR spectra, combined with quantitative analysis of magnetic susceptibilities, confirmed that the manganese is substitutionally incorporated into the ZnO nanocrystals as Mn 2+ with very homogeneous speciation, differing from bulk Mn 2+ :ZnO only in the magnitude of D-strain. Robust ferromagnetism was observed in spin-coated thin films of the nanocrystals, with 300 K saturation moments as large as 1.35 µ B /Mn 2+ and T C > 350 K. A distinct ferromagnetic resonance signal was observed in the EPR spectra of the ferromagnetic films. The occurrence of ferromagnetism in Mn 2+ :ZnO and its dependence on synthetic variables are discussed in the context of these and previous theoretical and experimental results.
“…It was argued 15 that Mn-O-Mn clusters are favorable even at relatively lower doping level of Mn. Although Mn 2+ ions can substitute Zn 2+ sites homogeneously in the dilute limit, 10 the isolated state of Mn 2+ is destroyed due to substitutional occupation of the nearest Zn 2+ sites by other Mn 2+ ions for increasing concentration of Mn.…”
“…This effect was accounted for by different sites of Mn ions in the host lattice [8] as well as their interaction with Zn i [2,5,13] and V O [1][2][3][4][5]. The possibility of Mn cluster formation also should be taken into account [6,27]. To elucidate the influence of native defects on Mn-related emission in ZnO:Mn ceramics further investigations are planned.…”
Abstract. Defect related emission in undoped and doped with manganese ZnO ceramics was investigated. Mn concentration N Mn was varied from 10 19 to 10 21 cm -3.The samples were sintered for 3 hours in air at 1100 °C. The color of ZnO:Mn ceramics changed from yellow to reddish-brown with increasing the Mn content. Photoluminescence (PL) spectra of prepared samples were measured at room temperature and analyzed by Gaussian fitting. PL of undoped ceramics exhibited itself as intense broad band peaking at about 550 nm. Two effects were shown to occur as a result of Mn doping: i) drastic quenching of self-activated PL accompanied by gradual red-shift of spectral boundary of the quenching with increasing the Mn content; ii) appearance of a new emission band peaking at 645 nm that becomes dominant in the PL spectrum at N Mn = 10 20 cm -3 . The observed effects were believed to be due to re-absorption of self-activated ZnO emission by Mn-related centers. The following recombination in excited centers was supposed to occur by both radiative and nonradiative ways, the former being responsible for 645 nm PL band.
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